Gene Name |
splicing regulatory glutamine/lysine-rich protein 1 |
heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A) |
Image |
No pdb structure |
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Gene Ontology Annotations |
Cellular Component |
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Molecular Function |
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Biological Process |
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Pathways |
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Drugs |
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Diseases |
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GWAS |
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Protein-Protein Interactions |
55 interactors:
CD8A
CSNK2A1
DDX17
DDX39B
DDX3X
DGKA
DGKD
EFTUD2
ELAVL1
GNB2L1
HNRNPA1
HNRNPA2B1
HNRNPA3
HNRNPC
HNRNPD
HNRNPH1
HNRNPK
HNRNPU
ILF2
MDM2
NCL
NPM1
PABPC1
PABPC4
PARP1
PIN1
RBM10
RBMX
SAFB
SF3A3
SF3B3
SFPQ
SH3GLB2
SNRPD1
SNRPD3
SRPK1
SRPK2
SRPK3
SRSF1
SRSF10
SRSF11
SRSF2
SRSF3
SRSF4
SRSF5
SRSF6
SRSF7
SRSF8
SSRP1
SUPT16H
TARBP1
THRAP3
TRA2B
YBX1
ZRANB2
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35 interactors:
ACTB
BTRC
CASP3
CD5
CDKN2A
CR2
ELL
EP300
ERG
GAS7
GRIN1
GRIN2D
GTF2H1
HNRNPD
HNRNPH3
IL7R
KAT2B
NDN
NDRG1
NEDD4
NR3C1
PIN1
POLR2A
POU3F4
PRMT1
PRPF40A
PTPN11
SMN1
SREK1
STAU1
SYK
TCERG1
WBP4
YAP1
ZNF689
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Entrez ID |
140890 |
3192 |
HPRD ID |
18043 |
04185 |
Ensembl ID |
ENSG00000153914
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ENSG00000153187
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Uniprot IDs |
E5RFV3
Q8WXA9
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Q00839
Q96BA7
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PDB IDs |
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1ZRJ
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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17p13
1q21
1q44
2q23
2q31
agilent
annotations
asd
autism
backgrounds
cgh
cnv
cnvs
disabilities
dissect
encephalopathy
epileptic
exome
expand
hallux
implicates
infantile
intellectual
lissencephaly
mbd5
microcephaly
pafah1b1
pathogenicity
spasms
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Tagcloud (Difference) ? |
|
17p13
1q21
1q44
2q23
2q31
agilent
annotations
asd
autism
backgrounds
cgh
cnv
cnvs
disabilities
dissect
encephalopathy
epileptic
exome
expand
hallux
implicates
infantile
intellectual
lissencephaly
mbd5
microcephaly
pafah1b1
pathogenicity
spasms
|
Tagcloud (Intersection) ? |
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